G93.41
BillableMetabolic encephalopathy
Metabolic encephalopathy
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Septic encephalopathy
Excludes 2
Conditions not included here, but the patient may have both
- certain conditions originating in the perinatal period (P04-P96)
- certain infectious and parasitic diseases (A00-B99)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
- alcoholic encephalopathy (G31.2)
- encephalopathy in diseases classified elsewhere (G94)
- hypertensive encephalopathy (I67.4)
- toxic (metabolic) encephalopathy (G92.8)
Also Known As / Clinical Terms
SNOMED CT
- Uraemic encephalopathy35145002
- Uremic encephalopathy35145002
- Hyperaminoaciduria42930003
- Inborn error of amino acid metabolism42930003
- Metabolic brain syndrome50122000
- Metabolic encephalopathy50122000
- Hyperglycinaemia64654004
- Hyperglycinemia64654004
- Complication of haemodialysis85223007
- Complication of hemodialysis85223007
- DDS - dialysis disequilibrium syndrome87235005
- Dialysis disequilibrium87235005
- Dialysis disequilibrium syndrome87235005
- Dialysis dysequilibrium syndrome87235005
- Deficiency of dioxygenase124234008
- Myxedema encephalopathy192816007
- Myxoedema encephalopathy192816007
- Urate encephalopathy230357002
- Hyponatraemic encephalopathy230358007
- Hyponatremic encephalopathy230358007
- Secondary amyloid encephalopathy230359004
- Acute disorder of haemodialysis236538004
- Acute disorder of hemodialysis236538004
- HD - Acute complications of haemodialysis236538004
- HD - Acute complications of hemodialysis236538004
- Disorder of glycine cleavage enzyme complex237939006
- NKH - Non-ketotic hyperglycinaemia237939006
- NKH - Non-ketotic hyperglycinemia237939006
- Non ketotic hyperglycinaemia237939006
- Non ketotic hyperglycinemia237939006
- Non-ketotic hyperglycinaemia237939006
- Non-ketotic hyperglycinemia237939006
- 3-Methylglutaconic aciduria type 4297233004
- Glucose transporter protein type 1 deficiency syndrome445252005
- Mitochondrial encephalomyopathy447292006
- Mitochondrial myoencephalopathy447292006
- 3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome711409002
- 3-methylglutaconic aciduria with deafness, encephalopathy, Leigh-like syndrome711409002
- 3-methylglutaconic aciduria with hearing loss, encephalopathy, Leigh-like syndrome711409002
- MEGDEL syndrome711409002
- Encephalopathy due to sulfite oxidase deficiency715980003
- Encephalopathy due to sulphite oxidase deficiency715980003
- Mitochondrial encephalocardiomyopathy due to transmembrane protein 70 mutation718212006
- TMEM70 related mitochondrial encephalo-cardio-myopathy718212006
- Mitochondrial neurogastrointestinal encephalomyopathy syndrome718214007
- Mitochondrial encephalomyopathy due to COXPD6 deficiency722212004
- Mitochondrial encephalomyopathy due to combined oxidative phosphorylation deficiency 6722212004
- Severe X-linked mitochondrial encephalomyopathy722212004
- Ethylmalonic encephalopathy723307008
- Thiamine-responsive encephalopathy723557004
- Progressive polyneuropathy with bilateral striatal necrosis771305006
- Childhood encephalopathy due to thiamin pyrophosphokinase deficiency773668008
- Childhood encephalopathy due to thiamine pyrophosphokinase deficiency773668008
- Asparagine synthetase deficiency782757004
- Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome782757004
- Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency783734000
- Mitochondrial deoxyribonucleic acid depletion syndrome, hepatocerebral form due to deoxyguanosine kinase deficiency783734000
- Atypical glycine encephalopathy1156791007
- Atypical non-ketotic hyperglycinaemia1156791007
- Atypical non-ketotic hyperglycinemia1156791007
- Infantile glycine encephalopathy1156826003
- Infantile non-ketotic hyperglycinaemia1156826003
- Infantile non-ketotic hyperglycinemia1156826003
- Recurrent metabolic encephalomyopathic crises, rhabdomyolysis, cardiac arrhythmia, intellectual disability syndrome1172698005
- TANGO2-related metabolic encephalopathy, arrhythmia syndrome1172698005
- Transport and golgi organisation 2 homolog-related metabolic encephalopathy, arrhythmia syndrome1172698005
- Transport and golgi organization 2 homolog-related metabolic encephalopathy, arrhythmia syndrome1172698005
- Encephalopathy with sepsis1204463009
- Sepsis-associated encephalopathy1204463009
- Sepsis-associated mental obtundation1204463009
- Septic encephalopathy1204463009
- ITPA-related lethal infantile neurological disorder with cataract and cardiac involvement1208747005
- Inosine triphosphate pyrophosphohydrolase-related lethal infantile neurological disorder with cataract and cardiac involvement1208747005
- Martsolf-like syndrome1208747005
- Encephalopathy due to mitochondrial and peroxisomal fission defect1236807002
- Acute reversible leucoencephalopathy due to SLC13A3 deficiency1340040004
- Acute reversible leucoencephalopathy due to sodium-dependent dicarboxylate transporter deficiency1340040004
- Acute reversible leucoencephalopathy with increased urinary alpha-ketoglutarate1340040004
- Acute reversible leukoencephalopathy due to SLC13A3 deficiency1340040004
- Acute reversible leukoencephalopathy due to sodium-dependent dicarboxylate transporter deficiency1340040004
- Acute reversible leukoencephalopathy with increased urinary alpha-ketoglutarate1340040004
- Ethylmalonic encephalopathy protein 1 deficiency821000124103
UMLS
- Associated Encephalopathies, SepsisC0393642
- Associated Encephalopathy, SepsisC0393642
- Encephalopathies, Sepsis AssociatedC0393642
- Encephalopathies, Sepsis-AssociatedC0393642
- Encephalopathy with sepsisC0393642
- Encephalopathy with sepsis (disorder)C0393642
- Encephalopathy, Sepsis AssociatedC0393642
- Encephalopathy, Sepsis-AssociatedC0393642
- Sepsis Associated EncephalopathiesC0393642
- Sepsis Associated EncephalopathyC0393642
- Sepsis-Associated EncephalopathiesC0393642
- Sepsis-Associated EncephalopathyC0393642
- Sepsis-associated encephalopathyC0393642
- Sepsis-associated mental obtundationC0393642
- Septic encephalopathyC0393642
- BRAIN DIS METABC0006112
- BRAIN SYNDROME METABC0006112
- Brain Disease, MetabolicC0006112
- Brain Diseases, MetabolicC0006112
- Brain Disorder, MetabolicC0006112
- Brain Disorders, MetabolicC0006112
- Brain Metabolic DisorderC0006112
- Brain Metabolic DisordersC0006112
- Brain Syndrome, MetabolicC0006112
- ENCEPH METABC0006112
- Encephalopathies, MetabolicC0006112
- Encephalopathy, MetabolicC0006112
- METAB BRAIN DISC0006112
- METAB BRAIN SYNDROMEC0006112
- METAB BRAIN SYNDROMESC0006112
- METAB DIS BRAINC0006112
- METAB ENCEPHC0006112
- Metabolic Brain DiseaseC0006112
- Metabolic Brain DiseasesC0006112
- Metabolic Brain DisorderC0006112
- Metabolic Brain DisordersC0006112
- Metabolic Brain SyndromeC0006112
- Metabolic Brain SyndromesC0006112
- Metabolic Disorder, BrainC0006112
- Metabolic Disorders, BrainC0006112
- Metabolic EncephalopathiesC0006112
- Metabolic EncephalopathyC0006112
- Metabolic brain syndromeC0006112
- Metabolic encephalopathyC0006112
- Metabolic encephalopathy (disorder)C0006112
- Metabolic encephalopathy NOSC0006112
- encephalopathy metabolicC0006112
- metabolic brain diseasesC0006112
- metabolic disorders brainC0006112
- metabolic encephalopathyC0006112
Frequently Asked Questions
What is the ICD-10 code for metabolic encephalopathy?
The ICD-10-CM code for metabolic encephalopathy is G93.41. The full clinical description is "Metabolic encephalopathy". G93.41 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code G93.41 mean?
ICD-10-CM code G93.41 represents "Metabolic encephalopathy". It is classified under Chapter 6: Diseases of the Nervous System and is a billable/specific code that can be used on a claim.
Is G93.41 a billable code?
Yes, G93.41 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G93.41 in?
G93.41 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What SNOMED CT codes does G93.41 map to?
G93.41 maps to 35 SNOMED CT concepts: 297233004, 711409002, 236538004, 1340040004, 782757004, and 30 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for G93.41?
G93.41 is linked to 2 UMLS Concept Unique Identifiers: C0393642, C0006112. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.